EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS003-26027 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr2:71275970-71278280 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7606102chr271276399hg19
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr27127667171277515
chr27127599171276191
chr27127624571276295
chr27127712771277224
Number: 1             
IDChromosomeStartEnd
GH02I071047chr27127466971277473
Enhancer Sequence
GGGTTTCATA GACTGTGGAT CCCAAACTTT GCAGTATTAG CCAAGCCTTT GTATGACCTC 60
ACAAAGTTTG GGGGTGGGGG GACAGGGAAA CTTTTGAATG CGGATCCCAA CAACAGCAAG 120
CCTTTCATGA GTTAAAGGAA AAACTTATGT CAGCCCCAGC CCTGGGGCTA CCCGATCTGA 180
CAAAGCCTTT TACATTGTAT GTGTCAGAAA GAGAAAAGAT GGCAGTTGGA GTTTTAAGCC 240
AAACTGTGGG GCCCTGGCCG AGGCCGGTGG CCTACCTCTC TAAACAACTA GATGGAGTTT 300
CTAAAGGATG GCCCCCCTGT TTGAGGGCCT TGGCAGCAAC TGCCCTGCTA GTCCAAGAAG 360
CAAATAAGCT GACTTTTGGG CAAAACCTGA ACATAAAGGC CCCCCATGTT GGGGTGACTT 420
TAATGAACAC TAAAGGACAT CATTGGCTAA TGAATGCTAG ACTCATCAAG TACCAAAGTG 480
TGCTCTGTGA AAATCCCCGT ATAACCACTG AAGTTTGTAA CACCCTAAAC CCTGCCACCT 540
TGCTCCCGGT ATCAGAGCGG CCTGTCAAGC GTGATTGTGT AGAAGTGTTG GATTCAGTTG 600
ACTCTAGCAG ACCTGACCTT CGGGACCAGC CTTGGGCATC AGTAGACTGG GAACTATACG 660
TGGACAGGAG CAGCTTCATC AACCCACAAG GAGAGAGATG TGCAGGATAT ACAGTGATGC 720
AGTAGTAGCC CTGGATACTG TTGTTGAAGC CAGATCATTG CCCCAGGCCA CTTCAGCCCA 780
GAAAACTGAA CTCATTGCTT TAATTGGGGC CTTAGAACTC AGTGAAGGTG AGACTGTCAA 840
CATTGACACT GATTCTCGGT ATGCCTTTTT AACCCTTCAA GTGCGTAGAG GATTATAGAA 900
AGAAAAGGGC CTACTGAACT CTGGGGGGAA AGACATAAAA TATCAACAAG AAATCTTGCA 960
ATTATTAGAA GCAGTATGGA AACCCCACAA GGTGGCACTT AGGCATCAGC AAGCTTCCAC 1020
CTTGCTGGGT TTGGGGAATT CCCACGCTGA CTCAGAGGCT CAAAAAGCAG CATCTGTCCC 1080
CTTCCAGGCA TCAGTCACAG CCCCTCTGCT CCCTCAAACA CCTGATCTTG TACCTACTTC 1140
TTCTAAAGAA GAAAAGGACT TTCTCCAGGT AAAGGGGAGG ACAAGTGACA GAGGAAGGAT 1200
GGATTCAGTT ACCAGATGGG AGAGTAGCTG TGCCACAGCT CCTAGGAGGT GCAGTTGTAC 1260
TGGCTGTGCA TGAAACCATC CATCTAGGTC AGGAGTCACT GGAAAAGTTG TTAGGCCGGT 1320
ATTTCTACAT CTCGCATTTG TCAGCCCTCG CCAAAACCAT GAGGCAGCGG TTTGTTACCT 1380
GCCGACACCA TAATGCGAGG CAAGGTCCAG CTGTTCCGCC CGGCATACAA GCTTATGCAG 1440
CAGCCCCCAT TGAAGATCTG CAGGTAGACT TCAGAGAGAT GCCAAAGTGT GGAGGTAACA 1500
AGTATTTACT AGTTCTTGGG TGTACCTAGT CTGGGTGGGT GGAGGCTTAT CCAACATGAA 1560
CTGAGAAAGC TCGTGAAGTA ACCCATCTGC TTCTTCGAGA TCTTATTCCT AGGTTTGAAC 1620
TGCCCTTATG GGTAGGCTCA GATAACGGGC CAGTGTTTGT GGCTGACTTG GTACAGAAGA 1680
CGGCAAAGGT ATTGGGGATC ACACGGAAAC TGCATGCCGC CTCCCAGCCT CAGAGTTCCG 1740
GAAAGGTGGA GCGGATGAAT CGGACTATCA AAAATAGTGC TATACTATTG TCTTCCCCGC 1800
TGGATATTTA AAACAGCACC ACAAGGGGCA TCAAACCACC TGCTAAATTT GAGGGAATGT 1860
TATCCTCTCC CCACCTCCCC CGGCCCCGGA TATTAGAGAC AATAACACAG GGGTAATGTA 1920
CACCCACTGC TTTATTGGGA GTAATATCAT CCTCTCCCTT CTTGGATATT AGGAACAATA 1980
TCACACTGTG CATGTACGCC TGTCGTGAAA TTCAATGGAA TGTCATCCTT TGCCTCCCTG 2040
GATATGATGA ACAATATCAC GGGGGATGTA CAACTTGTGA GATATTGGGA GTGATATCAT 2100
CCTCTCCCGT CTGGAAGTTA GGGACAGTAT CACAGGGGTG GTGTACACCC TCTGGGATGT 2160
TGGGACTAAT ATCATCCTCC CGCCCACTGG ATATGAAAAA CCATATCACA AGGGGCTTGT 2220
ACACACACTT CGATATTGGT ATTAATACCA TCCTCTCCCT CTTTGGATAT TCGGTGCCAT 2280
ATTTCAGGTG GGGTATACAC CACCTGCAAT 2310